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GC-MS Analysis, Antioxidant, Antidiabetic Activity, and ADMET Study of Diospyros mespiliformis Hochst. Ex A. DC. Ebenaceae Stembark

Yıl 2024, Cilt: 44 Sayı: 3, 198 - 219, 01.09.2024
https://doi.org/10.52794/hujpharm.1356537

Öz

The present study carried out GC-MS analysis, antioxidant, antidiabetic, and ADMET study of the crude ethanol extract (CRE), ethyl acetate (EAF), and aqueous (AQF) fractions of Diospyros mespiliformis (DM). Grandiflorenic and cis, cis-linoleic acids were the most abundant of the 59 and 40 compounds identified in the EAF and AQF, respectively. The EAF and CRE exhibited significantly (p< 0.05) higher total antioxidant capacity than the AQF. Furthermore, the EAF exhibited a significantly (p < 0.05) higher percentage inhibition via the ferric thiocyanate assay than the CRE and AQF. All the extracts showed significantly (p < 0.05) lower malondialdehyde concentrations than AA in the thiobarbituric acid assay. Diazoprogesterone identified in the EAF exhibited the lowest binding affinity and inhibition constant, interacting with myeloperoxidase (MPO), xanthine (XO), and 11-β-hydroxysteroid dehydrogenase (HSD1), and sirtuin 6 (SIRT6). The molecular dynamics simulations showed residue fluctuations of the diazoprogesterone docked complexes with the highest observed at Ser42, Cys1325, Ser281, and Leu78 for MPO, XO, HSD1, and SIRT6, respectively. Moreover, diazoprogesterone was predicted to possess good ADMET properties. Conclusively, DM possesses significant antioxidant and antidiabetic potential, containing compounds that might be a source of novel therapeutics against oxidative stress and diabetes.

Destekleyen Kurum

Tertiary Education Trust Fund of Nigeria

Kaynakça

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GC-MS Analizi, Antioksidan, Antidiyabetik Aktivite ve Diospyros mespiliformis Hochst'un ADMET Çalışması. Eski A. DC. Ebenaceae Sap Kabuğu

Yıl 2024, Cilt: 44 Sayı: 3, 198 - 219, 01.09.2024
https://doi.org/10.52794/hujpharm.1356537

Öz

The present study carried out GC-MS analysis, antioxidant, antidiabetic, and ADMET study of the crude ethanol extract (CRE), ethyl acetate (EAF), and aqueous (AQF) fractions of Diospyros mespiliformis (DM). Grandiflorenic (25.36%) and cis, cis-linoleic (27.13%) acids were the most abundant of the 59 and 40 compounds identified in the EAF and AQF, respectively. The EAF and CRE exhibited total antioxidant capacity of 77.78 ±0.01 ascorbic acid equivalent (mg AAE/g extract) and 60.20 ±0.01 mg AAE/g extract, respectively, significantly (p < 0.05) than the AQF (29.63 ±0.01 mg AAE/g extract). Furthermore, the EAF (38.27% ±2.44) exhibited a significantly (p < 0.05) higher percentage inhibition via the ferric thiocyanate assay than the CRE (17.45% ±2.18) and AQF (15.91% ±2.11). All the extracts showed significantly (p < 0.05) lower malondialdehyde concentrations than AA in the thiobarbituric acid assay. Additionally, the AQF exhibited a significantly higher percentage of H2O2 scavenging than the AA and EAF at 100 µg/ml. Diazoprogesterone (compound III) identified in the EAF exhibited the lowest respective binding affinity and inhibition constant, interacting with myeloperoxidase (-9 kcal/mol and 0.25 µM), xanthine oxidase (-9.9 kcal/mol and 0.05 µM), 11-β-hydroxysteroid dehydrogenase (-10 kcal/mol and 0.05µM), and sirtuin 6 (-10 kcal/mol and 0.05 µM). The molecular dynamics simulations showed residue fluctuations of the diazoprogesterone-docked complexes with the highest observed at Ser42 (5.14 Å), Cys1325 (8.96 Å), Ser281 (7.71 Å), and Leu78 (3.91 Å) for myeloperoxidase, xanthine oxidase, 11-β-hydroxysteroid dehydrogenase, and sirtuin 6, respectively compared to the undocked targets. Moreover, diazoprogesterone was predicted to possess good ADMET properties. Conclusively, DM possesses significant antioxidant and antidiabetic potential, containing compounds that might be a source of novel therapeutics against oxidative stress and diabetes.

Kaynakça

  • 1. American Diabetes Association Professional Practice Committee. Classification and Diagnosis of Diabetes: Standards of Medical Care in Diabetes—2022. Diabetes Care. 2022;45(1):S17-S38. https://doi.org/10.2337/dc22-s002
  • 2. Bhatti JS, Sehrawat A, Mishra J, Sidhu IS, Navik U, Khullar N, et al. Oxidative stress in the pathophysiology of type 2 diabetes and related complications: Current therapeutics strategies and future perspectives. Free Radical Biol Med. 2022;184:114-34. https://doi.org/10.1016/j.freeradbiomed.2022.03.019
  • 3. Domingueti CP, Dusse LMSA, Carvalho MdG, de Sousa LP, Gomes KB, Fernandes AP. Diabetes mellitus: The linkage between oxidative stress, inflammation, hypercoagulability and vascular complications. J Diabetes Complications. 2016;30(4):738-45. https://doi.org/10.1016/j. jdiacomp.2015.12.018
  • 4. Giacco F, Brownlee M. Oxidative stress and diabetic complications. Circul Res. 2010;107(9):1058-70. https://doi. org/10.1161/circresaha.110.223545
  • 5. Pasupuleti VR, Arigela CS, Gan SH, Salam SKN, Krishnan KT, Rahman NA, et al. A Review on Oxidative Stress, Diabetic Complications, and the Roles of Honey Polyphenols. Oxid Med Cell Longev. 2020;2020:8878172. https://doi. org/10.1155/2020/8878172
  • 6. Adwas AA, Elsayed A, Azab AE, Quwaydir FA. Oxidative stress and antioxidant mechanisms in human body. J Appl Biotechnol Bioeng. 2019;6(1):43-7. https://doi.org/10.15406/ jabb.2019.06.00173
  • 7. Ali SS, Ahsan H, Zia MK, Siddiqui T, Khan FH. Understanding oxidants and antioxidants: Classical team with new players. J Food Biochem. 2020;44(3):e13145. https://doi.org/10.1111/ jfbc.13145
  • 8. Hayes JD, Dinkova-Kostova AT, Tew KD. Oxidative Stress in Cancer. Cancer Cell. 2020;38(2):167-97. https://doi. org/10.1016/j.ccell.2020.06.001
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  • 11. Naris S. Significant Role of Free Radicals in Diabetes Mellitus. Oxidants and Antioxidants in Medical Science. 2022;11(08):1- 2.
  • 12. Dahiru MM, Alfa MB, Abubakar MA, Abdulllahi AP. Assessment of in silico antioxidant, anti-inflammatory, and antidiabetic activites of Ximenia americana L. Olacaceae. Advances in Medical, Pharmaceutical and Dental Research. 2024;4(1):1-13. http://dx.doi.org/10.21622/ AMPDR.2024.04.1.735
  • 13. Dahiru MM, Musa N. Phytochemical Profiling, Antioxidant, Antidiabetic, and ADMET Study of Diospyros mespiliformis Leaf, Hochst Ex A. Dc Ebenaceae. J Fac Pharm Ankara/ Ankara Ecz Fak Derg. 2024;48(2):412-35. http://dx.doi. org/10.33483/jfpau.1354293
  • 14. Dahiru MM, Musa N, Abaka AM, Abubakar MA. Potential Antidiabetic Compounds from Anogeissus leiocarpus: Molecular Docking, Molecular Dynamic Simulation, and ADMET Studies. Borneo J Pharm. 2023;6(3):249-77. https:// doi.org/10.33084/bjop.v6i3.5027
  • 15. Heitaku S, Sasase T, Sotani T, Maki M, Katsumi S, Fukuda S, et al. An 11-beta hydroxysteroid dehydrogenase type 1 inhibitor, JTT-654 ameliorates insulin resistance and non-obese type 2 diabetes. Biol Pharm Bull. 2023;46(7):969-78. https://doi. org/10.1248/bpb.b23-00129
  • 16. Morgan SA, Gathercole LL, Hassan-Smith ZK, Tomlinson J, Stewart PM, Lavery GG. 11β-HSD1 contributes to age-related metabolic decline in male mice. J Endocrinol. 2022;255(3):117-29. https://doi.org/10.1530/joe-22-0169
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  • 35. Muhammad NB, Wasagu RSU, Sani B. Effect of Methanolic Extract of African Ebony (Diospyros mespiliformis) Stem Bark on Liver and Kidney Function Biomarkers in Alloxan Induced Diabetic Albino Rats. Asian J Biochem Genet Mol Biol. 2020;6(3):51-5. https://doi.org/10.9734/ajbgmb/2020/ v6i330156
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Toplam 69 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Eczacılık Biyokimyası, Farmasotik Kimya
Bölüm Research Articles
Yazarlar

Muhammad Mubarak Dahıru 0000-0002-1252-3699

Neksumi Musa 0000-0003-1389-021X

Yayımlanma Tarihi 1 Eylül 2024
Kabul Tarihi 8 Temmuz 2024
Yayımlandığı Sayı Yıl 2024 Cilt: 44 Sayı: 3

Kaynak Göster

Vancouver Dahıru MM, Musa N. GC-MS Analysis, Antioxidant, Antidiabetic Activity, and ADMET Study of Diospyros mespiliformis Hochst. Ex A. DC. Ebenaceae Stembark. HUJPHARM. 2024;44(3):198-219.